| NDC Code | 45802-238-65 |
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| Package Description | 30 TABLET, FILM COATED in 1 BOTTLE (45802-238-65) |
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| Product NDC | 45802-238 |
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| Product Type Name | HUMAN PRESCRIPTION DRUG |
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| Proprietary Name | Alogliptin And Pioglitazone |
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| Non-Proprietary Name | Alogliptin Benzoate And Pioglitazone Hydrochloride |
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| Dosage Form | TABLET, FILM COATED |
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| Usage | ORAL |
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| Start Marketing Date | 20160408 |
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| Marketing Category Name | NDA AUTHORIZED GENERIC |
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| Application Number | NDA022426 |
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| Manufacturer | Padagis Israel Pharmaceuticals Ltd |
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| Substance Name | ALOGLIPTIN BENZOATE; PIOGLITAZONE HYDROCHLORIDE |
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| Strength | 12.5; 15 |
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| Strength Unit | mg/1; mg/1 |
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| Pharmacy Classes | Dipeptidyl Peptidase 4 Inhibitor [EPC], Dipeptidyl Peptidase 4 Inhibitors [MoA], PPAR alpha [CS], PPAR gamma [CS], Peroxisome Proliferator Receptor alpha Agonist [EPC], Peroxisome Proliferator Receptor gamma Agonist [EPC], Peroxisome Proliferator-activated Receptor Activity [MoA], Thiazolidinedione [EPC], Thiazolidinediones [CS] |
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